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抑制刺猬信号通路通过扰乱细胞周期延缓肝脏再生。

Inhibition of Hedgehog Delays Liver Regeneration through Disrupting the Cell Cycle.

作者信息

Tao Jiawang, Chen Yan, Zhuang Yuanqi, Wei Ruzhi, Getachew Anteneh, Pan Tingcai, Yang Fan, Li Yinxiong

机构信息

Institute of Public Health, Guangzhou Institutes of Biomedicine and Health (GIBH), Chinese Academy of Sciences (CAS), Guangzhou 510530, China.

University of Chinese Academy of Sciences, Beijing 100049, China.

出版信息

Curr Issues Mol Biol. 2022 Jan 18;44(2):470-482. doi: 10.3390/cimb44020032.

Abstract

Liver regeneration is a complicated biological process orchestrated by various liver resident cells. Hepatic cell proliferation and reconstruction of the hepatic architecture involve multiple signaling pathways. It has been reported that the Hh signal is involved in liver regeneration. However, the signal transduction pathways and cell types involved are ill studied. This study aimed to investigate hedgehog signal response cell types and the specific molecular mechanism involved in the process of liver regeneration. Partial hepatectomy (PH) of 70% was performed on ICR (Institute of Cancer Research) mice to study the process of liver regeneration. We found that the hedgehog signal was activated significantly after PH, including hedgehog ligands, receptors and intracellular signaling molecules. Ligand signals were mainly expressed in bile duct cells and non-parenchymal hepatic cells, while receptors were expressed in hepatocytes and some non-parenchymal cells. Inhibition of the hedgehog signal treated with vismodegib reduced the liver regeneration rate after partial hepatectomy, including inhibition of hepatic cell proliferation by decreasing Cyclin D expression and disturbing the cell cycle through the accumulation of Cyclin B. The current study reveals the important role of the hedgehog signal and its participation in the regulation of hepatic cell proliferation and the cell cycle during liver regeneration. It provides new insight into the recovery of the liver after liver resection.

摘要

肝脏再生是一个由多种肝脏驻留细胞精心编排的复杂生物学过程。肝细胞增殖和肝脏结构重建涉及多个信号通路。据报道,Hh信号参与肝脏再生。然而,所涉及的信号转导途径和细胞类型研究较少。本研究旨在探究刺猬信号反应细胞类型以及肝脏再生过程中涉及的具体分子机制。对ICR(癌症研究所)小鼠进行70%的部分肝切除术(PH)以研究肝脏再生过程。我们发现,PH后刺猬信号被显著激活,包括刺猬信号配体、受体和细胞内信号分子。配体信号主要在胆管细胞和非实质肝细胞中表达,而受体在肝细胞和一些非实质细胞中表达。用维莫德吉抑制刺猬信号降低了部分肝切除术后的肝脏再生率,包括通过降低细胞周期蛋白D的表达抑制肝细胞增殖以及通过细胞周期蛋白B的积累扰乱细胞周期。当前研究揭示了刺猬信号的重要作用及其在肝脏再生过程中参与肝细胞增殖和细胞周期调控的过程。它为肝切除术后肝脏的恢复提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3806/8928988/2c0c897b0dca/cimb-44-00032-g001.jpg

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